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MeSH keywords -> Related genes, diseases (OMIM)


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01 IgA Deficiency [NCBI]

Gene


 Gene Link Information
Gain		 01
IGAD1 [NCBI] 0.000854821
IGAN [NCBI] 8.93865e-05
TNFRSF13B [NCBI] 8.88854e-05
TNFSF13B [NCBI] 2.68412e-05
TNFSF13 [NCBI] 1.99894e-05
NBN [NCBI] 1.45168e-05
BTK [NCBI] 1.41968e-05
HLA-B [NCBI] 1.33352e-05
TNF [NCBI] 1.23859e-05
MSH5 [NCBI] 1.18236e-05
HLA-DQB1 [NCBI] 1.17318e-05
IL10 [NCBI] 1.10086e-05
HLA-DRA [NCBI] 9.54036e-06
TNFRSF13C [NCBI] 9.06198e-06
TGM2 [NCBI] 7.91249e-06
AFP [NCBI] 7.89095e-06
MAP3K14 [NCBI] 7.79497e-06
PTPN22 [NCBI] 6.95078e-06
TAP2 [NCBI] 6.62913e-06
AMBP [NCBI] 6.26429e-06
TAP1 [NCBI] 6.17462e-06
HLA-DQA1 [NCBI] 5.90773e-06
HLA-A [NCBI] 5.86635e-06
HLA-DRB1 [NCBI] 4.05243e-06
IL6 [NCBI] 3.77777e-06



OMIM


 OMIM Link Information
gain		 01
IGAD1 [NCBI] 0.010087
CVID [NCBI] 0.00269164
ocular motor apraxia [NCBI] 0.00056504
pulmonary alveolar proteinosis, acquired [NCBI] 0.000528242
CD [NCBI] 0.000389034
TNFRSF13B [NCBI] 0.000210686
IGAD2 [NCBI] 0.000187762
HIGM1 [NCBI] 0.000179672
ataxia-telangiectasia with generalized skin pigmentation and early death [NCBI] 0.000116222
MSH5 [NCBI] 9.09049e-05
BTK [NCBI] 8.59254e-05
CHH [NCBI] 8.53892e-05
IGHG2 [NCBI] 7.71252e-05
IGLC1 [NCBI] 6.60373e-05
IFNG [NCBI] 4.96058e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 4.72104e-05
BLM [NCBI] 3.08448e-05
MBL2 [NCBI] 2.67493e-05
AFP [NCBI] 2.44558e-05
RA [NCBI] 2.43933e-05
TNF [NCBI] 2.05968e-05
TTR [NCBI] 1.82998e-05
SLE [NCBI] 1.38342e-05
AT [NCBI] 1.01137e-05
CEACAM5 [NCBI] 2.60153e-06



Database Center for Life Science